Abstract
Nod1 is an intracellular protein that is involved in recognition
of bacterial molecules and whose genetic variation has been
linked to several inflammatory diseases. Previous studies suggested
that the recognition core of Nod1 stimulatory molecules
is -D-glutamyl-meso-diaminopimelic acid (iE-DAP), but the
identity of the major Nod1 stimulatory molecule produced by
bacteria remains unknown. Here we show that bacteria produce
lipophilic molecules capable of stimulating Nod1. Analysis of
synthetic compounds revealed stereoselectivity of the DAP residue
and that conjugation of lipophilic acyl residues specifically
enhances the Nod1 stimulatory activity of the core iE-DAP. Furthermore,
we demonstrate that lipophilic molecules induce
and/or enhance the secretion of innate immune mediators from
primary mouse mesothelial cells and human monocytic Mono-
Mac6 cells, and this effect is mediated through Nod1. These
results provide insight into the mechanism of immune recognition
via Nod1, which might be useful in the design and testing of
novel immunoregulators.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 11757-11764 |
| Number of pages | 8 |
| Journal | Journal of Biological Chemistry |
| Volume | 282 |
| Issue number | 16 |
| Publication status | Published - 2007 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
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